Standard

IgG levels

IGHG1 · rs10136766

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of IgG levels compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with IgG levels.
G/G Published research associates this genotype with typical/baseline likelihood of IgG levels — no copies of the reported risk allele.
Source

Questions about rs10136766

What is rs10136766?

rs10136766 is a single position in the genome, in or near the IGHG1 gene. Published research associates it with igg levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10136766 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs10136766 come from?

GWAS Catalog, Ann Neurol 2012, PMID:23225573. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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